Canonical Allele Identifier: CA3435341

Gene: STING1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.139478334T>C , CM000667.2:g.139478334T>C	GRCh38
NC_000005.9:g.138857919T>C , CM000667.1:g.138857919T>C	GRCh37
NC_000005.8:g.138838103T>C	NCBI36
NG_034249.1:g.9457A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000330794.9:c.695A>G MANE Select	ENSP00000331288.4:p.His232Arg
ENST00000502362.2:n.1470A>G
ENST00000510817.2:c.695A>G	ENSP00000427455.2:p.His232Arg
ENST00000511886.6:n.1637A>G
ENST00000512606.6:n.931A>G
ENST00000514119.6:n.914A>G
ENST00000650883.1:c.*112A>G	ENSP00000499142.1:n.*112A>G
ENST00000651565.1:c.338A>G	ENSP00000498768.1:p.His113Arg
ENST00000651699.1:c.695A>G	ENSP00000499166.1:p.His232Arg
ENST00000652110.1:c.695A>G	ENSP00000498513.1:p.His232Arg
ENST00000652271.1:c.695A>G	ENSP00000498596.1:p.His232Arg
ENST00000652293.1:n.1503A>G
ENST00000652543.1:c.338A>G	ENSP00000498683.1:p.His113Arg
ENST00000652640.1:n.1269A>G
ENST00000330794.8:c.695A>G	ENSP00000331288.4:p.His232Arg
ENST00000502825.1:n.473A>G
ENST00000503287.5:n.587A>G
ENST00000507297.5:n.2028A>G
ENST00000509573.5:n.494A>G
ENST00000510817.1:c.695A>G	ENSP00000427455.1:p.His232Arg
ENST00000511886.5:n.701A>G
ENST00000512606.5:n.620A>G
NM_001301738.1:c.695A>G	NP_001288667.1:p.His232Arg
NM_198282.3:c.695A>G	NP_938023.1:p.His232Arg
XM_005268445.2:c.695A>G	XP_005268502.1:p.His232Arg
XM_011537639.1:c.695A>G	XP_011535941.1:p.His232Arg
XM_011537640.1:c.338A>G	XP_011535942.1:p.His113Arg
XM_005268445.4:c.695A>G	XP_005268502.1:p.His232Arg
XM_011537639.3:c.695A>G	XP_011535941.1:p.His232Arg
XM_011537640.2:c.338A>G	XP_011535942.1:p.His113Arg
NM_001301738.2:c.695A>G	NP_001288667.1:p.His232Arg
NM_001367258.1:c.338A>G	NP_001354187.1:p.His113Arg
NM_198282.4:c.695A>G MANE Select	NP_938023.1:p.His232Arg